Canonical Allele Identifier: CA127213070

Gene: SLC22A5

Linked Data

• dbSNP Id: rs976955675
• MyVariant Identifiers: chr5:g.131729404G>T (hg19) ; chr5:g.132393712G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393712G>T , CM000667.2:g.132393712G>T	GRCh38
NC_000005.9:g.131729404G>T , CM000667.1:g.131729404G>T	GRCh37
NC_000005.8:g.131757303G>T	NCBI36
NG_008982.1:g.29004G>T
NG_008982.2:g.29009G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-473G>T	ENSP00000388838.2:n.1292-473G>T
ENST00000435065.7:c.1559G>T	ENSP00000402760.2:p.Gly520Val
ENST00000448810.6:c.*339G>T	ENSP00000401860.2:n.*339G>T
ENST00000685543.1:n.1628G>T
ENST00000686757.1:c.*651G>T	ENSP00000510721.1:n.*651G>T
ENST00000686868.1:n.479G>T
ENST00000687740.1:n.4172G>T
ENST00000688151.1:n.2797G>T
ENST00000689271.1:c.1334G>T	ENSP00000510797.1:p.Gly445Val
ENST00000690900.1:c.*651G>T	ENSP00000510703.1:n.*651G>T
ENST00000692212.1:n.4627G>T
ENST00000692355.1:c.740G>T
ENST00000692413.1:c.1469G>T	ENSP00000509374.1:p.Gly490Val
ENST00000692825.1:c.1555G>T	ENSP00000509447.1:n.1555G>T
ENST00000693308.1:c.1535G>T	ENSP00000509770.1:p.Gly512Val
ENST00000693763.1:n.2647G>T
ENST00000245407.8:c.1487G>T MANE Select	ENSP00000245407.3:p.Gly496Val
ENST00000245407.7:c.1487G>T	ENSP00000245407.3:p.Gly496Val
ENST00000435065.6:c.1559G>T	ENSP00000402760.2:p.Gly520Val
ENST00000447841.5:c.331G>T
ENST00000448810.5:c.749G>T
ENST00000461013.5:n.8909G>T
ENST00000475308.1:n.2165G>T
NM_001308122.1:c.1559G>T	NP_001295051.1:p.Gly520Val
NM_003060.3:c.1487G>T	NP_003051.1:p.Gly496Val
XM_011543590.1:c.869G>T	XP_011541892.1:p.Gly290Val
XR_948290.1:n.1613G>T
XM_011543590.2:c.869G>T	XP_011541892.1:p.Gly290Val
XM_017009778.2:c.959G>T	XP_016865267.1:p.Gly320Val
XR_001742215.1:n.1742G>T
XR_001742216.1:n.1761G>T
XR_427718.2:n.1847G>T
XR_948290.2:n.1613G>T
XR_948291.2:n.1841G>T
NM_003060.4:c.1487G>T MANE Select	NP_003051.1:p.Gly496Val
NM_001308122.2:c.1559G>T	NP_001295051.1:p.Gly520Val